FDA Inspection 1044834 — Carmen F. Castellano, OD

Carmen F. Castellano, OD — FEI 3014140952

The FDA completed an inspection of Carmen F. Castellano, OD on Mar 5, 2018 in Saint Louis, MO. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Mar 5, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Saint Louis, MO (United States)

Additional Details

Clinical Investigator (CI)